Ponticaepoxide

Details

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Internal ID 282fddb9-d9fa-48c7-af76-1b52d8c5ea7e
Taxonomy Organoheterocyclic compounds > Epoxides
IUPAC Name (2R,3R)-2-ethenyl-3-[(E)-non-1-en-3,5,7-triynyl]oxirane
SMILES (Canonical) CC#CC#CC#CC=CC1C(O1)C=C
SMILES (Isomeric) CC#CC#CC#C/C=C/[C@@H]1[C@H](O1)C=C
InChI InChI=1S/C13H10O/c1-3-5-6-7-8-9-10-11-13-12(4-2)14-13/h4,10-13H,2H2,1H3/b11-10+/t12-,13-/m1/s1
InChI Key ZJMXHGIVVFPAJY-HRFIDBLHSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H10O
Molecular Weight 182.22 g/mol
Exact Mass 182.073164938 g/mol
Topological Polar Surface Area (TPSA) 12.50 Ų
XlogP 2.60
Atomic LogP (AlogP) 1.53
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Ponticaepoxide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9876 98.76%
Caco-2 - 0.5764 57.64%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Lysosomes 0.3800 38.00%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9038 90.38%
OATP1B3 inhibitior + 0.9642 96.42%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9510 95.10%
P-glycoprotein inhibitior - 0.9566 95.66%
P-glycoprotein substrate - 0.8973 89.73%
CYP3A4 substrate - 0.5153 51.53%
CYP2C9 substrate + 0.8110 81.10%
CYP2D6 substrate - 0.8113 81.13%
CYP3A4 inhibition - 0.9480 94.80%
CYP2C9 inhibition - 0.7334 73.34%
CYP2C19 inhibition + 0.5059 50.59%
CYP2D6 inhibition - 0.9559 95.59%
CYP1A2 inhibition - 0.5000 50.00%
CYP2C8 inhibition - 0.9129 91.29%
CYP inhibitory promiscuity - 0.6255 62.55%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5344 53.44%
Carcinogenicity (trinary) Non-required 0.4069 40.69%
Eye corrosion + 0.7975 79.75%
Eye irritation - 0.7370 73.70%
Skin irritation + 0.6936 69.36%
Skin corrosion + 0.5441 54.41%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6512 65.12%
Micronuclear - 0.6800 68.00%
Hepatotoxicity + 0.6678 66.78%
skin sensitisation + 0.6756 67.56%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity - 0.8000 80.00%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity + 0.6478 64.78%
Acute Oral Toxicity (c) II 0.5568 55.68%
Estrogen receptor binding - 0.7161 71.61%
Androgen receptor binding - 0.7316 73.16%
Thyroid receptor binding - 0.5524 55.24%
Glucocorticoid receptor binding - 0.5993 59.93%
Aromatase binding - 0.5139 51.39%
PPAR gamma - 0.6343 63.43%
Honey bee toxicity - 0.5810 58.10%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.6737 67.37%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL3227 P41594 Metabotropic glutamate receptor 5 93.20% 96.42%
CHEMBL1951 P21397 Monoamine oxidase A 85.39% 91.49%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 81.97% 94.80%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 80.58% 95.58%
CHEMBL226 P30542 Adenosine A1 receptor 80.10% 95.93%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Artemisia annua
Artemisia carvifolia

Cross-Links

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PubChem 102368592
NPASS NPC37702